Clinical Trial Administrator

Institution/Unit: Nuffield Department of Population Health, University of Oxford

Salary:  £32,332 - £38,205

Closing date: 26-07-2024

Details:

Oxford Population Health (Nuffield Department of Population Health) contains world-renowned population health research groups and provides an excellent environment for multi-disciplinary research and teaching. The Clinical Trial Service Unit (CTSU) is a major international research institute within the NDPH, and is one of the world’s leading centres for research into chronic diseases, such as cancer and heart disease. As Clinical Trial Administrator, you will support the Senior Clinical Trial Managers and the multi-disciplinary Trials Senior Management Team (SMT) with the administration of the study, with particular emphasis on ensuring agreed study milestones are met and the day-to-day operational aspects of the study run smoothly, playing a key role in troubleshooting any problems that might arise. To be considered for the Clinical Trial Administrator post, you will have a University degree, relevant administrative and data management experience with the ability to work accurately, paying close attention to detail. You will also have excellent organisational and communication skills and the ability to work cohesively and effectively as part of a busy team. The post is full time (part time considered) and fixed term 2 years. The closing date for applications is noon on Friday 26 July 2024

More information: 

For more information, and for how to apply, please see the Job page

Project Manager

Institution/Unit:  Oxford University Department of Paediatrics

Salary: £36,024 - £44,263

Closing date: 12-08-2024

Details:

The Oxford Vaccine Group (OVG) are seeking a Project Manager to primarily support and manage the delivery of CEPI funded Nipah programme, which includes clincal and vaccine manufacturing. The Project Manager, will work both as a member of a multi-disciplinary team and independently, using their initiative to seek solutions to problems and provide excellent administrative support. Considerable experience in coordinating and project management of complex projects, thorough working knowledge of legislative, finance and research governance requirements and vaccine manufacturing. The ideal candidate will have excellent interpersonal and management skills and be able to interact productively and accurately with other team members, researchers and collaborators. While this collaborative approach will be a key feature of your role, you will also be required to work independently, taking the lead in initiatives. You will be able to handle a demanding and varied workload, managing your time and prioritising your work effectively. Postholders will have experience in setting up, delivering translational clinical research, ensuring that both day to day project coordination and activities are completed to a high standard. They will need to be highly organised, able to deal with complex information, and able to prioritise a varied workload to meet deadlines. Previous experience in project management in vaccinology/immunology is preferred for this position.

More information:

Fore more information, and for how to apply, please see the Job page

Project Administrator

Institution/Unit: NDORMS, Oxford Trauma and Emergency Care

Salary: £28,759 - £33,966 p.a.

Closing date: 09-08-2024

Details:

We have an exciting opportunity for a Project Administrator to join the Oxford Trauma group at the Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, to be based at the Kadoorie Critical Care Centre, John Radcliffe Hospital, Oxford. As a Project Administrator, you will carry out day-to-day administrative coordination of project(s) with minimum supervision, reporting problems immediately, and providing updates to the Trial Manager. You will work within the Oxford Clinical Trials Research Unit (OCTRU) Standard Operating Procedures (SOPs). You will be responsible for monitoring of your own project and related junior staff to ensure quality assurance compliance and you will provide administrative support for meetings and support to the Trial Manager in the development of case report forms and documents

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For more information, and for how to apply, please see the Job page


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